{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Stafford Springs",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90456",
      "recalling_firm": "Hobbs Medical, Inc.",
      "address_1": "8 Spring St",
      "address_2": "N/A",
      "postal_code": "06076-1505",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.",
      "recall_number": "Z-1388-2022",
      "product_description": "Hobbs Medical Polypectomy Snare, Catalog No. 7202",
      "product_quantity": "45 (US)",
      "reason_for_recall": "During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band. Kinking of the sheath may prevent the snare from fully closing, and injury may result.",
      "recall_initiation_date": "20220603",
      "center_classification_date": "20220715",
      "report_date": "20220727",
      "code_info": "UDI-DI: M84972020 Package UDI: M84972021 Lots: H11-20-017 H04-20-062 H04-19-056 H11-19-077 H08-17-014R H10-17-089R H10-17-089 H0S-17-014 H06-17-167"
    }
  ]
}